@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_head
{
this:
np:hasAssertion
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion
;
np:hasProvenance
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance
;
np:hasPublicationInfo
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion
a
np:Assertion
.
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance
a
np:Provenance
.
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion
{
miriam-gene:3811
a
ncit:C16612
.
lld:C0018133
a
ncit:C7057
.
dgn-gda:DGN32f195d2786c543241f65638a136514d
sio:SIO_000628
miriam-gene:3811
,
lld:C0018133
;
a
sio:SIO_001121
.
}
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance
{
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion
dcterms:description
"[Our study suggests that KIR genotyping of donor and recipient pairs could contribute to the identification of patients at high risk for developing severe complications of haematopoietic SCT and thus may help with the choice of intensity of GVHD prophylaxis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:20173792
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}